Site Research Assistant - Grenoble job opportunity at IQVIA Holdings, Inc..

Home Jobs In France Tag: Job Site Research Assistant - Grenoble position at IQVIA Holdings, Inc.


DatePosted 17 Days Ago bot
IQVIA Holdings, Inc. Site Research Assistant - Grenoble
Experience: 2-years
Pattern: part-time
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loacation Grenoble, France, France
loacation Grenoble, Fran..........France

Are you looking for an opportunity to work with an industry-leading company? IQVIA is currently recruiting for a Site Research Assistant to support a site in Grenoble. This role with an start beginning of April is for 16 hours per week and is expected to last around 6 months. The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies, under the direction and delegation of the Principal Investigator. As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support the clinical trial team and ensure the smooth running of the clinical trial, including: Maintaining up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents Support with screening and enrolment of patients and collection of related documents (informed consent, privacy consent, etc.); Planning and coordinating logistical activity for study procedures according to the study protocol Data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness Management and shipment of biological samples Coordinating with study monitor on study issues and effectively responding to monitor-initiated questions Administrative research task We are looking for candidates with: BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, Research Assistant, nurse, medical assistant, other medical profession Good knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules Must have at least 1-2 years experience working as a Clinical Research Assistant or Clinical Research Coordinator at a clinical trial site Basic knowledge of medical terminology Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and clients Good organizational skills with the ability to pay close attention to detail Fluent French language skills ​ If this sounds like the perfect opportunity for you, please apply now! #LI-Onsite #LI-DNP  #LI-CES  #LI-NS1 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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